EP3464248B1 - 3-oxo-2,6-diphényl-2,3-dihydropyridazine-4-carboxamides - Google Patents

3-oxo-2,6-diphényl-2,3-dihydropyridazine-4-carboxamides Download PDF

Info

Publication number
EP3464248B1
EP3464248B1 EP17724833.3A EP17724833A EP3464248B1 EP 3464248 B1 EP3464248 B1 EP 3464248B1 EP 17724833 A EP17724833 A EP 17724833A EP 3464248 B1 EP3464248 B1 EP 3464248B1
Authority
EP
European Patent Office
Prior art keywords
oxo
dihydropyridazine
carboxamide
fluorophenyl
chlorophenyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP17724833.3A
Other languages
German (de)
English (en)
Other versions
EP3464248A1 (fr
Inventor
Norbert Schmees
Ilona GUTCHER
Horst Irlbacher
Benjamin Bader
Na Zhao
Michael Platten
Ulrike Roehn
Ludwig Zorn
Lars Roese
Detlef Stoeckigt
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Deutsches Krebsforschungszentrum DKFZ
Bayer Pharma AG
Original Assignee
Deutsches Krebsforschungszentrum DKFZ
Bayer Pharma AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Deutsches Krebsforschungszentrum DKFZ, Bayer Pharma AG filed Critical Deutsches Krebsforschungszentrum DKFZ
Publication of EP3464248A1 publication Critical patent/EP3464248A1/fr
Application granted granted Critical
Publication of EP3464248B1 publication Critical patent/EP3464248B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/14—Oxygen atoms
    • C07D237/16—Two oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/20—Nitrogen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • the present invention covers 3-oxo-2,6-diphenyl-2,3-dihydropyridazine-4-carboxamide compounds of general formula (I) as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment of diseases, in particular cancer or conditions with dysregulated immune responses, as a sole agent or in combination with other active ingredients.
  • the AHR (Aryl Hydrocarbon Receptor) is a ligand-activated transcription factor, belonging to the basic helix-loop-helix/Per-Arnt-Sim (bHLH/PAS) family, and is located in the cytosol. Upon ligand binding, the AHR translocates to the nucleus where it heterodimerises with ARNT (AHR Nuclear Translocator) upon which it interacts with DREs (Dioxin Response Elements) of AHR-responsive genes to regulate their transcription.
  • ARNT AHR Nuclear Translocator
  • DREs Dioxin Response Elements
  • the AHR is best known for binding to environmental toxins and inducing the metabolic machinery, such as cytochrome P 450 enzymes (eg.
  • CYP1A1, CYP1A2 and CYP1B1 required for their elimination ( Reyes et al., Science, 1992, 256(5060):1193-5 ).
  • Activation of AHR by xenobiotics has demonstrated its role in numerous cellular processes such as embryogenesis, tumourigenesis and inflammation.
  • AHR is expressed in many cells of the immune system, including dendritic cells (DCs), macrophages, T cells and NK cells, and plays an important role in immunoregulation ( Nguyen et al., Front Immunol, 2014, 5:551 ).
  • AHR activation promotes regulatory T cell generation, inhibits Th1 and Th17 differentiation, directly and indirectly, and decreases the activation and maturation of DCs ( Wang et al., Clin Exp Immunol, 2014, 177(2):521-30 ; Mezrich et al., J Immunol, 2010, 185(6): 3190-8 ; Wei et al., Lab Invest, 2014, 94(5):528-35 ; Nguyen et al., PNAS, 2010, 107(46):19961-6 ).
  • AHR activation modulates the innate immune response and constitutive AHR expression has been shown to negatively regulate the type-I interferon response to viral infection ( Yamada et al., Nat Immunol, 2016 ). Additionally, mice with a constitutively active AHR spontaneously develop tumours ( Andersson et al., PNAS, 2002, 99(15):9990-5 ). In addition to xenobiotics, the AHR can also bind metabolic products of tryptophan degradation.
  • Tryptophan metabolites such as kynurenine and kynurenic acid
  • AHR ligands that activate the AHR under physiological conditions
  • Other endogenous ligands are known to bind the AHR although their physiological roles are currently unknown ( Nguyen & Bradfield, Chem Res Toxicol, 2008, 21(1):102-116 ).
  • immunosuppressive properties of kynurenine and tryptophan degradation are well described and are implicated in cancer-associated immunosuppression.
  • the enzymes indoleamine-2,3-dioxygenases 1 and 2 (IDO1/IDO2) as well as tryptophan-2,3-dioxygenase 2 (TDO2) are responsible for catalysing the first and rate-limiting step of tryptophan metabolism.
  • IDO1/2-mediated degradation of tryptophan in tumours and tumour-draining lymph nodes reduces anti-tumour immune responses and inhibition of IDO can suppress tumour formation in animal models ( Uyttenhove et al., Nat Med, 2003, 9(10):1269-74 ; Liu et al., Blood, 2005, 115(17): 3520-30 ; Muller et al., Nat Med, 11(3):312-9 ; Metz, Cancer Res, 2007, 67(15):7082-7 ).
  • TDO2 is also strongly expressed in cancer and can lead to the production of immunosuppressive kynurenine.
  • tumour growth In glioma, activation of the AHR by kynurenine, downstream of TDO-mediated tryptophan degradation, enhances tumour growth as a consequence of inhibiting anti-tumour immune responses as well as directly promoting tumour cell survival and motility ( Opitz et al., Nature, 2011, 478(7368):197-203 ).
  • AHR ligands generated by tumour cells therefore act in both an autocrine and paracrine fashion on tumour cells and lymphocytes, respectively, to promote tumour growth.
  • the present invention covers 3-oxo-2,6-diphenyl-2,3-dihydropyridazine-4-carboxamide compounds of general formula (I) which inhibit the AHR.
  • WO 2010/059401 relates to compounds and compositions for expanding the number of CD34+ cells for transplantation.
  • WO 2010/059401 relates inter alia to heterocyclic compounds capable of down-regulating the activity and/or expression of AHR.
  • WO 2012/015914 relates to compositions and methods for modulating AHR activity.
  • WO 2012/015914 relates inter alia to heterocyclic compounds that modulate AHR activity for use in therapeutic compositions.
  • WO 2007/058392 relates to novel heterocyclic compounds and a pharmaceutical use thereof.
  • WO 2007/058392 relates inter alia to heterocyclic compounds having an hepatitis C virus cell infection inhibitory activity.
  • WO 2002/022587 relates to novel compounds exhibiting inhibitory activities against AMPA receptor and/or kainate receptor.
  • WO 2002/022587 relates inter alia to pyridazinone and triazinone compounds.
  • US 5,418,233 relates to heterobiaryl derivatives inhibiting cell-cell aggregation and cell-matrix interactions.
  • US 5,418,233 relates to heterobiaryl derivatives which are histamine receptor antagonists.
  • WO 2015/143164 relates to antimicrobial agents and screening methods.
  • WO 2015/143164 relates inter alia to pyridazinone compounds as antibiotics.
  • WO 2009/142732 relates to substituted pyridazinone derivatives and their use as H 3 antagonists/inverse agonists.
  • the state of the art does not describe the 3-oxo-2,6-diphenyl-2,3-dihydropyridazine-4-carboxamide compounds of general formula (I) of the present invention as described and defined herein.
  • the compounds of the present invention have surprising and advantageous properties.
  • the compounds of the present invention have surprisingly been found to effectively inhibit AHR for which data are given in biological experimental section and may therefore be used for the treatment or prophylaxis of cancer or other conditions where exogenous and endogenous AHR ligands induce dysregulated immune responses, uncontrolled cell growth, proliferation and/or survival of tumour cells, immunosuppression in the context of cancer, inappropriate cellular immune responses, or inappropriate cellular inflammatory responses or diseases which are accompanied with uncontrolled cell growth, proliferation and/or survival of tumour cells, immunosuppression in the context of cancer inappropriate cellular immune responses, or inappropriate cellular inflammatory responses, particularly in which the uncontrolled cell growth, proliferation and/or survival of tumour cells, immunosuppression in the context of cancer, inappropriate cellular immune responses, or inappropriate cellular inflammatory responses is mediated by AHR, such as, for example, liquid and solid tumours, and/or metastases thereof, e.g.
  • AHR such as, for example, liquid and solid tumours, and/or metastases
  • tumours of the thorax including non-small cell and small cell lung tumours, gastrointestinal tumours including colon, colorectal and pancreatic tumours, liver tumours, endocrine tumours, mammary and other gynecological tumours, urological tumours including renal, bladder and prostate tumours, skin tumours, and sarcomas, and/or metastases thereof.
  • the present invention covers compounds of general formula (I): in which
  • substituted means that one or more hydrogen atoms on the designated atom or group are replaced with a selection from the indicated group, provided that the designated atom's normal valency under the existing circumstances is not exceeded. Combinations of substituents and/or variables are permissible.
  • optionally substituted means that the number of substituents can be equal to or different from zero. Unless otherwise indicated, it is possible that optionally substituted groups are substituted with as many optional substituents as can be accommodated by replacing a hydrogen atom with a non-hydrogen substituent on any available carbon atom. Commonly, it is possible for the number of optional substituents, when present, to be 1, 2 or 3.
  • comprising when used in the specification includes “consisting of”.
  • halogen means a fluorine, chlorine, bromine or iodine, particularly a fluorine, chlorine or bromine atom.
  • C 2 -C 8 -alkyl means a linear or branched, saturated, monovalent hydrocarbon group having 2, 3, 4, 5, 6, 7 or 8 carbon atoms, e.g.
  • said group has 2, 3 or 4 carbon atoms ("C 2 -C 4 -alkyl”), e.g. a ethyl, propyl, isopropyl, butyl, sec-butyl isobutyl, or tert -butyl group, more particularly 2 or 3 carbon atoms (“C 2 -C 3 -alkyl”), e.g. a ethyl, n-propyl or isopropyl group.
  • C 2 -C 4 -alkyl 2, 3 or 4 carbon atoms
  • C 2 -C 8 -hydroxyalkyl means a linear or branched, saturated, monovalent hydrocarbon group in which the term “C 2 -C 8 -alkyl” is defined supra, and in which 1 or 2 hydrogen atoms are replaced with a hydroxy group, e.g .
  • C 1 -C 4 -alkoxy means a linear or branched, saturated, monovalent group of formula (C 1 -C 4 -alkyl)-O-, which means methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy or tert- butoxy .
  • C 3 -C 6 -cycloalkyl means a saturated, monovalent, monocyclic hydrocarbon ring which contains 3, 4, 5 or 6 carbon atoms (“C 3 -C 6 -cycloalkyl”). Said C 3 -C 6 -cycloalkyl group is a monocyclic hydrocarbon ring, e.g. a cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
  • 4- to 6-membered heterocycloalkyl means a monocyclic, saturated heterocycle with 4, 5 or 6 ring atoms in total, which contains one or two identical or different ring heteroatoms from the series N, O and S, it being possible for said heterocycloalkyl group to be attached to the rest of the molecule via any one of the carbon atoms or, if present, a nitrogen atom.
  • Said heterocycloalkyl group can be a 4-membered ring, such as azetidinyl, oxetanyl or thietanyl, for example; or a 5-membered ring, such as tetrahydrofuranyl, 1,3-dioxolanyl, thiolanyl, pyrrolidinyl, imidazolidinyl, pyrazolidinyl, 1,1-dioxidothiolanyl, 1,2-oxazolidinyl, 1,3-oxazolidinyl or 1,3-thiazolidinyl, for example; or a 6-membered ring, such as tetrahydropyranyl, tetrahydrothiopyranyl, piperidinyl, morpholinyl, dithianyl, thiomorpholinyl, piperazinyl, 1,3-dioxanyl, 1,4-dioxanyl or 1,2-
  • 4- to 6-membered heterocycloalkyl means a 4- to 6-membered heterocycloalkyl as defined supra containing one ring oxygen atom and optionally one further ring heteroatom from the series: N, O, S.
  • 5- or 6-membered heterocycloalkyl means a monocyclic, saturated heterocycle with 5 or 6 ring atoms in total, containing one ring oxygen atom.
  • monocyclic heteroaryl means a monovalent, aromatic ring having 5 or 6 ring atoms (a “5- or 6-membered heteroaryl” group), which contains at least one ring heteroatom and optionally one or two further ring heteroatoms from the series: N, O and/or S, and which is bound via a ring carbon atom or optionally via a ring nitrogen atom (if allowed by valency).
  • Said heteroaryl group can be a 5-membered heteroaryl group, such as, for example, thienyl, furanyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, triazolyl, thiadiazolyl or tetrazolyl; or a 6-membered heteroaryl group, such as, for example, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl or triazinyl.
  • a 5-membered heteroaryl group such as, for example, thienyl, furanyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, triazolyl, thiadiazolyl
  • the heteroaryl or heteroarylene groups include all possible isomeric forms thereof, e.g .: tautomers and positional isomers with respect to the point of linkage to the rest of the molecule.
  • the term pyridinyl includes pyridin-2-yl, pyridin-3-yl and pyridin-4-yl; or the term thienyl includes thien-2-yl and thien-3-yl.
  • the heteroaryl group is a imidazolyl group.
  • stable compound' or “stable structure” is meant a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.
  • the compounds of the present invention optionally contain one or more asymmetric centres, depending upon the location and nature of the various substituents desired.
  • one or more asymmetric carbon atoms are present in the (R) or (S) configuration, which can result in racemic mixtures in the case of a single asymmetric centre, and in diastereomeric mixtures in the case of multiple asymmetric centres.
  • asymmetry also be present due to restricted rotation about a given bond, for example, the central bond adjoining two substituted aromatic rings of the specified compounds.
  • Preferred compounds are those which produce the more desirable biological activity.
  • Separated, pure or partially purified isomers and stereoisomers or racemic or diastereomeric mixtures of the compounds of the present invention are also included within the scope of the present invention. The purification and the separation of such materials can be accomplished by standard techniques known in the art.
  • Preferred isomers are those which produce the more desirable biological activity.
  • These separated, pure or partially purified isomers or racemic mixtures of the compounds of this invention are also included within the scope of the present invention.
  • the purification and the separation of such materials can be accomplished by standard techniques known in the art.
  • the optical isomers can be obtained by resolution of the racemic mixtures according to conventional processes, for example, by the formation of diastereoisomeric salts using an optically active acid or base or formation of covalent diastereomers. Examples of appropriate acids are tartaric, diacetyltartaric, ditoluoyltartaric and camphorsulfonic acid.
  • Mixtures of diastereoisomers can be separated into their individual diastereomers on the basis of their physical and/or chemical differences by methods known in the art, for example, by chromatography or fractional crystallisation.
  • the optically active bases or acids are then liberated from the separated diastereomeric salts.
  • a different process for separation of optical isomers involves the use of chiral chromatography (e.g ., HPLC columns using a chiral phase), with or without conventional derivatisation, optimally chosen to maximise the separation of the enantiomers.
  • Suitable HPLC columns using a chiral phase are commercially available, such as those manufactured by Daicel, e.g ., Chiracel OD and Chiracel OJ, for example, among many others, which are all routinely selectable. Enzymatic separations, with or without derivatisation, are also useful.
  • the optically active compounds of the present invention can likewise be obtained by chiral syntheses utilizing optically active starting materials.
  • the present invention includes all possible stereoisomers of the compounds of the present invention as single stereoisomers, or as any mixture of said stereoisomers, e.g . (R)- or (S)-isomers, in any ratio.
  • Isolation of a single stereoisomer, e.g . a single enantiomer or a single diastereomer, of a compound of the present invention is achieved by any suitable state of the art method, such as chromatography, especially chiral chromatography, for example.
  • the compounds of the present invention can exist as N-oxides, which are defined in that at least one nitrogen of the compounds of the present invention is oxidised.
  • the present invention includes all such possible N-oxides.
  • the present invention also covers useful forms of the compounds of the present invention, such as metabolites, hydrates, solvates, salts, in particular pharmaceutically acceptable salts, and/or co-precipitates.
  • the compounds of the present invention can exist as a hydrate, or as a solvate, wherein the compounds of the present invention contain polar solvents, in particular water, methanol or ethanol for example, as structural element of the crystal lattice of the compounds.
  • the amount of polar solvents, in particular water it is possible for the amount of polar solvents, in particular water, to exist in a stoichiometric or non-stoichiometric ratio.
  • stoichiometric solvates e.g . a hydrate, hemi-, (semi-), mono-, sesqui-, di-, tri-, tetra-, penta- etc. solvates or hydrates, respectively.
  • the present invention includes all such hydrates or solvates.
  • the compounds of the present invention to exist in free form, e.g . as a free base, or as a free acid, or as a zwitterion, or to exist in the form of a salt.
  • Said salt may be any salt, either an organic or inorganic addition salt, particularly any pharmaceutically acceptable organic or inorganic addition salt, which is customarily used in pharmacy, or which is used, for example, for isolating or purifying the compounds of the present invention.
  • pharmaceutically acceptable salt refers to an inorganic or organic acid addition salt of a compound of the present invention. For example, see S. M. Berge, et al. "Pharmaceutical Salts," J. Pharm. Sci. 1977, 66, 1-19 .
  • a suitable pharmaceutically acceptable salt of the compounds of the present invention may be, for example, an acid-addition salt of a compound of the present invention bearing a nitrogen atom, in a chain or in a ring, for example, which is sufficiently basic, such as an acid-addition salt with an inorganic acid, or "mineral acid", such as hydrochloric, hydrobromic, hydroiodic, sulfuric, sulfamic, bisulfuric, phosphoric, or nitric acid, for example, or with an organic acid, such as formic, acetic, acetoacetic, pyruvic, trifluoroacetic, propionic, butyric, hexanoic, heptanoic, undecanoic, lauric, benzoic, salicylic, 2-(4-hydroxybenzoyl)-benzoic, camphoric, cinnamic, cyclopentanepropionic, digluconic, 3-hydroxy-2-naphthoic, nico
  • an alkali metal salt for example a sodium or potassium salt
  • an alkaline earth metal salt for example a calcium, magnesium or strontium salt, or an aluminium or a zinc salt
  • acid addition salts of the claimed compounds to be prepared by reaction of the compounds with the appropriate inorganic or organic acid via any of a number of known methods.
  • alkali and alkaline earth metal salts of acidic compounds of the present invention are prepared by reacting the compounds of the present invention with the appropriate base via a variety of known methods.
  • the present invention includes all possible salts of the compounds of the present invention as single salts, or as any mixture of said salts, in any ratio.
  • the present invention includes all possible crystalline forms, or polymorphs, of the compounds of the present invention, either as single polymorph, or as a mixture of more than one polymorph, in any ratio.
  • the invention further includes all possible crystallized and polymorphic forms of the inventive compounds, whereby the polymorphs are existing either as a single polymorph form or are existing as a mixture of several polymorphs in all concentrations.
  • the present invention covers compounds of general formula (I), supra, in which:
  • the present invention covers compounds of general formula (I), supra, in which: R 1 represents C 2 -C 6 -hydroxyalkyl, wherein said C 2 -C 6 -hydroxyalkyl groups are optionally substituted once with R 7 and optionally one to three times with halogen, or C 3 -C 6 -cycloalkyl substituted once with hydroxy; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 1 represents C 2 -C 6 -hydroxyalkyl, wherein said C 2 -C 6 -hydroxyalkyl groups are optionally substituted once with R 7 and optionally one to three times with halogen; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 1 represents C 3 -C 6 -cycloalkyl substituted once with hydroxy; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 1 represents C 5 -C 6 -cycloalkyl substituted once with hydroxy; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 2 represents chloro, methyl, fluoromethyl, difluoromethyl, trifluoromethyl, methoxy or difluoromethoxy; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 2 represents chloro, methyl or methoxy; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 3 represents hydrogen or methyl; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 4 represents hydrogen or halogen; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 4 represents hydrogen, fluoro or chloro; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 6 represents hydrogen or halogen; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 6 represents hydrogen, fluoro or chloro; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 6 represents hydrogen or fluoro; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 7 represents C 1 -C 4 -alkoxy, C 3 -C 6 -cycloalkyl, 4- to 6-membered heterocycloalkyl or monocyclic heteroaryl; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers compounds of general formula (I), supra, in which: R 7 represents methoxy, cyclopropyl, tetrahydrofuranyl, tetrahydropyranyl or imidazolyl; their polymorphs, enantiomeres, diastereomeres, racemates, tautomeres, N-oxides, hydrates and solvates, as well as their physiological acceptable salts and solvates of these salts, as well as mixtures of the same.
  • the present invention covers combinations of two or more of the above mentioned embodiments under the heading "further embodiments of the first aspect of the present invention".
  • the present invention covers any sub-combination within any embodiment or aspect of the present invention of compounds of general formula (I), supra.
  • the present invention covers any sub-combination within any embodiment or aspect of the present invention of intermediate compounds of general formula (VII).
  • the present invention covers the compounds of general formula (I) which are disclosed in the Example Section of this text, infra.
  • the compounds according to the invention of general formula (I) can be prepared according to the following scheme 1.
  • the scheme and procedures described below illustrate synthetic routes to the compounds of general formula (I) of the invention and are not intended to be limiting. It is clear to the person skilled in the art that the order of transformations as exemplified in scheme 1 can be modified in various ways. The order of transformations exemplified in this scheme is therefore not intended to be limiting. In addition, interconversion of any of the substituents R 1 , R 2 , R 3 , R 4 , R 5 or R 6 can be achieved before and/or after the exemplified transformations.
  • Scheme 1 shows a route for the preparation of compounds of general formula (I) in which R 1 , R 2 , R 3 , R 4 , R 5 and R 6 have the meaning as given for general formula (I), supra.
  • Ketomalonates represented as intermediates according to formula (III) are in some few instances commercially available or can be synthezised from alpha-halo-acetophenones (II) according to procedures known to persons skilled in the art.
  • Related alpha-halo-acetophenones are usually commercially available. Conversion of such alpha-halo-acteophenones with malonic acid esters in the presence of a suitable base in a suitable solvent results in the formation of non-commercial ketomalonates according to formula (III).
  • R in formula (III), (V) and (VI) represents a suitable alkyl group such as methyl, ethyl, propyl or other homologous groups.
  • a suitable solvent can be, but should not be restricted to, acetonitril, DMF, DMA, DMSO of THF, or even mixtures of these or other solvents.
  • a suitable base could be, but should not be restricted to, potassium carbonate, sodium hydride, caesium carbonate of potassium hexamethylendisilazane (see e.g.: J. Heterocycl. Chem., 25, (1988), p. 1689ff ; Med. Chem. Lett., 12, (2002), p. 1955 ff .; J. Med. Chem., 58, (2015), p. 3471 ff .).
  • Dihydropyrazinones according to formula (V) can be transferred to pyrazinones according to formula (VI). This can be accomplished by the use of a suitable reagents such as copper dichloride at elevated temperature ( Bioorg. Med. Chem. Lett., 21, (2011), P. 6362 ff .; Synthesis, (2003), p. 436 ff .; J. Med. Chem., 46, (2003), p. 349 ff .).
  • a suitable reagents such as copper dichloride at elevated temperature
  • the resulting pyrazinones according to formula (VI) with an ester functional group can be converted by methods known to the person skilled in the art, for example by basic hydrolysis with, for example, aqueous alkali metal hydroxides, or by acidic hydrolysis using, for example, hydrogen chloride in dioxane or trifluoroacetic acid, into the pyrazinone carboxylic acids (VII).
  • the present invention covers methods of preparing compounds of general formula (I) as defined supra, said methods comprising the step of allowing an intermediate compound of general formula (VII): in which
  • the compounds of the present invention can be administered as the sole pharmaceutical agent or in combination with one or more other pharmaceutically active ingredients where the combination causes no unacceptable adverse effects.
  • the present invention also covers such pharmaceutical combinations.
  • the compounds of the present invention can be combined with: 131I-chTNT, abarelix, abiraterone, aclarubicin, adalimumab, ado-trastuzumab emtansine, afatinib, aflibercept, aldesleukin, alectinib, alemtuzumab, alendronic acid, alitretinoin, altretamine, amifostine, aminoglutethimide, hexyl aminolevulinate, amrubicin, amsacrine, anastrozole, ancestim, anethole dithiolethione, anetumab ravtansine, angiotensin II, antithrombin III, aprepitant, arcitum
  • compositions comprising a PD-1/-L1 axis antagonist and an AHR antagonist and methods of using the same are provided herein.
  • Data presented herein demonstrate that a combination of AHR inhibition and blockade of the PD-1/-L1 axis reduces the growth of tumor cells in more than an additive manner.
  • PD-1 along with its ligands PD-L1 and PD-L2, function as negative regulators of T cell activation.
  • AHR suppresses immune cell function while increasing cancer cell proliferation and motility.
  • PD-L1 is overexpressed in many cancers and overexpression of PD-1 often occurs concomitantly in tumor infiltrating T cells.
  • compositions comprising a PD-1/-L1 axis antagonist and an AHR antagonist are surprisingly effective in enhancing an immune response and in the treatment of cancer.
  • inventive compounds can also be used as a therapeutic in a variety of other disorders wherein AHR is involved such as, cardiovascular and lung diseases.
  • the compounds according to the invention are suitable for the treatment and/or prophylaxis in particular of cardiovascular, inflammatory and fibrotic disorders and of renal disorders, in particular of acute and chronic renal insufficiency, and also of acute and chronic renal failure.
  • the compounds according to the invention can be used in medicaments for the treatment and/or prophylaxis of cardiovascular, inflammatory and fibrotic disorders, renal disorders, in particular of acute and chronic renal insufficiency, and also of acute and chronic renal failure.
  • renal insufficiency comprises both acute and chronic manifestations of renal insufficiency, and also underlying or related renal disorders such as diabetic and non-diabetic nephropathies, hypertensive nephropathies, ischaemic renal disorders, renal hypoperfusion, intradialytic hypotension, obstructive uropathy, renal stenoses, glomerulopathies, glomerulonephritis (such as, for example, primary glomerulonephritides; minimal change glomerulonephritis (lipoidnephrosis); membranous glomerulonephritis; focal segmental glomerulosclerosis (FSGS); membrane-proliferative glomerulonephritis; crescentic glomerulonephritis; mesangioproliferative glomerulonephritis (IgA nephritis, Berger's disease); post-infectious glomerulonephritis; secondary
  • the present invention also comprises the use of the compounds according to the invention for the treatment and/or prophylaxis of sequelae of renal insufficiency, for example pulmonary oedema, heart failure, uremia, anemia, electrolyte disturbances (for example hypercalemia, hyponatremia) and disturbances in bone and carbohydrate metabolism.
  • the present invention also comprises the use of the compounds according to the invention for the treatment and/or prevention of sequelae of renal insufficiency, for example pulmonary oedema, heart failure, uraemia, anaemia, electrolyte disturbances (for example hyperkalaemia, hyponatraemia) and disturbances in bone and carbohydrate metabolism.
  • the compounds according to the invention are further suitable for the treatment and/or prevention of polycystic kidney disease (PCKD) and of the syndrome of inappropriate ADH secretion (SIADH). Furthermore, the compounds according to the invention are also suitable for the treatment and/or prophylaxis of metabolic syndrome, hypertension, resistant hypertension, acute and chronic heart failure, coronary heart disease, stable and unstable angina pectoris, peripheral and cardiac vascular disorders, arrhythmias, atrial and ventricular arrhythmias and impaired conduction, for example atrioventricular blocks degrees I-III (AB block I-III), supraventricular tachyarrhythmia, atrial fibrillation, atrial flutter, ventricular fibrillation, ventricular flutter, ventricular tachyarrhythmia, Torsade de pointes tachycardia, atrial and ventricular extrasystoles, AV-junctional extrasystoles, sick sinus syndrome, syncopes, AV-nodal re-entry ta
  • the compounds according to the invention are also suitable for treatment and/or prophylaxis of asthmatic disorders, pulmonary arterial hypertension (PAH) and other forms of pulmonary hypertension (PH) including left-heart disease, HIV, sickle cell anaemia, thromboembolisms (CTEPH), sarcoidosis, COPD or pulmonary fibrosis-associated pulmonary hypertension, chronic-obstructive pulmonary disease (COPD), acute respiratory distress syndrome (ARDS), acute lung injury (ALI), alpha-1-antitrypsin deficiency (AATD), pulmonary fibrosis, pulmonary emphysema (for example pulmonary emphysema induced by cigarette smoke) and cystic fibrosis (CF).
  • PAH pulmonary arterial hypertension
  • PH pulmonary hypertension
  • COPD chronic-obstructive pulmonary disease
  • ARDS acute respiratory distress syndrome
  • ALI acute lung injury
  • AATD alpha-1-antitrypsin deficiency
  • CF
  • the compounds described in the present invention are also active compounds for control of central nervous system disorders characterized by disturbances of the NO/cGMP system. They are suitable in particular for improving perception, concentration, learning or memory after cognitive impairments like those occurring in particular in association with situations/diseases/syndromes such as mild cognitive impairment, age-associated learning and memory impairments, age-associated memory losses, vascular dementia, craniocerebral trauma, stroke, dementia occurring after strokes (post stroke dementia), post-traumatic craniocerebral trauma, general concentration impairments, concentration impairments in children with learning and memory problems, Alzheimer's disease, Lewy body dementia, dementia with degeneration of the frontal lobes including Pick's syndrome, Parkinson's disease, progressive dementia with corticobasal degeneration, amyolateral sclerosis (ALS), Huntington's disease, demyelinization, multiple sclerosis, thalamic degeneration, Creutzfeld-Jacob dementia, HIV dementia, schizophrenia with dementia or Korsakoff's psychosis.
  • the compounds according to the invention are also suitable for treatment and/or prophylaxis of central nervous system disorders such as states of anxiety, tension and depression, CNS-related sexual dysfunctions and sleep disturbances, and for controlling pathological disturbances of the intake of food, stimulants and addictive substances.
  • the compounds according to the invention are furthermore also suitable for controlling cerebral blood flow and thus represent effective agents for controlling migraines. They are also suitable for the prophylaxis and control of sequelae of cerebral infarction (cerebral apoplexy) such as stroke, cerebral ischaemia and craniocerebral trauma.
  • the compounds according to the invention can likewise be used for controlling states of pain and tinnitus.
  • the compounds according to the invention have anti-inflammatory action and can therefore be used as anti-inflammatory agents for treatment and/or prophylaxis of sepsis (SIRS), multiple organ failure (MODS, MOF), inflammatory disorders of the kidney, chronic intestinal inflammations (IBD, Crohn's disease, UC), pancreatitis, peritonitis, rheumatoid disorders, inflammatory skin disorders and inflammatory eye disorders.
  • SIRS sepsis
  • MODS multiple organ failure
  • IBD chronic intestinal inflammations
  • UC chronic intestinal inflammations
  • pancreatitis peritonitis
  • rheumatoid disorders inflammatory skin disorders and inflammatory eye disorders.
  • the compounds according to the invention can also be used for treatment and/or prophylaxis of autoimmune diseases.
  • the compounds according to the invention are also suitable for treatment and/or prophylaxis of fibrotic disorders of the internal organs, for example the lung, the heart, the kidney, the bone marrow and in particular the liver, and also dermatological fibroses and fibrotic eye disorders.
  • fibrotic disorders includes in particular the following terms: hepatic fibrosis, cirrhosis of the liver, pulmonary fibrosis, endomyocardial fibrosis, nephropathy, glomerulonephritis, interstitial renal fibrosis, fibrotic damage resulting from diabetes, bone marrow fibrosis and similar fibrotic disorders, scleroderma, morphea, keloids, hypertrophic scarring (also following surgical procedures), naevi, diabetic retinopathy, proliferative vitroretinopathy and disorders of the connective tissue (for example sarcoidosis).
  • the compounds according to the invention are also suitable for controlling postoperative scarring, for example as a result of glaucoma operations.
  • the compounds according to the invention can also be used cosmetically for ageing and keratinized skin.
  • the compounds according to the invention are suitable for treatment and/or prophylaxis of hepatitis, neoplasms, osteoporosis, glaucoma and gastroparesis.
  • the present invention further provides for the use of the compounds according to the invention for treatment and/or prophylaxis of disorders, especially the disorders mentioned above.
  • the present invention further provides for the use of the compounds according to the invention for the treatment and/or prophylaxis of chronic renal disorders, acute and chronic renal insufficiency, diabetic, inflammatory or hypertensive nephropaties, fibrotic disorders, cardiac insufficiency, angina pectoris, hypertension, pulmonary hypertension, ischemias, vascular disorders, thromboembolic disorders, arteriosclerosis, sickle cell anemia, erectile dysfunction, benign prostate hyperplasia, dysuria associated with benign prostate hyperplasia, Huntington, dementia, Alzheimer and Creutzfeld-Jakob.
  • the present invention further provides a method for treatment and/or prophylaxis of disorders, in particular the disorders mentioned above, using an effective amount of at least one of the compounds according to the invention.
  • the present invention further provides a method for the treatment and/or prophylaxis of chronic renal disorders, acute and chronic renal insufficiency, diabetic, inflammatory or hypertensive nephropathies, fibrotic disorders, cardiac insufficiency, angina pectoris, hypertension, pulmonary hypertension, ischemias, vascular disorders, thromboembolic disorders, arteriosclerosis, sickle cell anemia, erectile dysfunction, benign prostate hyperplasia, dysuria associated with benign prostate hyperplasia, Huntington, dementia, Alzheimer and Creutzfeld-Jakob.
  • the inventive compounds can also be used to treat or to prevent uterine fibroids (uterine leiomyoma or uterine myoma) in women.
  • Uterine fibroids are benign tumors of the myometrium, the smooth muscle layer of the uterus. Uterine fibroids grow slowly during a women's life, and their growth is dependent on the female sexual hormones estradiol and progesterone [ Kawaguchi K et al. Immunohistochemical analysis of oestrogen receptors, progesterone receptors and Ki-67 in leiomyoma and myometrium during the menstrual cycle and pregnancy Virchows Arch A Pathol Anat Histopathol.
  • TDO2 Tryptophan 2,3-dioxygenase, being highly upregulated [ Tsibris JC et al. Insights from gene arrays on the development and growth regulation of uterine leiomyomata. Fertil Steril. 2002 Jul;78(1):114-21 .]. TDO2 metabolizes the substrate L-Tryptophan to L-Kynurenine, which can be further metabolized to kynurenic acid.
  • L-Kynurenine and Kynurenic acid are physiological ligands and activators for the arylhydrocarbon receptor AHR [ Opitz CA et al. An endogenous tumour-promoting ligand of the human aryl hydrocarbon receptor Nature. 2011 Oct 5;478(7368):197-203 ].
  • L-Kynurenine controls at least two physiological processes which are dysregulated in uterine fibroids.
  • L-Kynurenine synthesized by an upregulation of IDO (Indoleamine-2,3-dyoxygenase) or TDO2, and acting via the AHR receptor, suppresses the immune system and thus prevents immune cells from recognizing and clearing the tumor cells [ Munn DH Blocking IDO activity to enhance anti-tumor immunity. Front Biosci (Elite Ed). 2012 Jan 1;4:734-45 ]. Furthermore, an upregulation of L-Kynurenine leads to a vasodilation of vessels, and thus can directly increase blood loss and bleeding [ Wang Y et al. Kynurenine is an endothelium-derived relaxing factor produced during inflammation Nature Medicine 16, 279-285 (2010 )].
  • Compounds of the present invention can be utilized to inhibit, block, reduce or decrease AHR activation by exogenous and/or endogenous ligands for the reduction of tumour growth and the modulation of dysregulated immune responses e.g. to block immunosuppression and increase immune cell activation and infiltration in the context of cancer and cancer immunotherapy;
  • This method comprises administering to a mammal in need thereof, including a human, an amount of a compound of this invention, or a pharmaceutically acceptable salt, isomer, polymorph, metabolite, hydrate, solvate or ester thereof; which is effective to treat the disorder.
  • the present invention also provides methods of treating a variety of other disorders wherein AHR is involved such as, but not limited to, inflammation, vaccination for infection & cancer, viral infections, obesity and diet-induced obesity, adiposity, metabolic disorders, hepatic steatosis and uterine fibroids.
  • treating or “treatment” as used in the present text is used conventionally, e.g., the management or care of a subject for the purpose of combating, alleviating, reducing, relieving, improving the condition of a disease or disorder, such as liquid and solid tumours.
  • the present invention covers compounds of general formula (I), as described supra, or stereoisomers, tautomers, N-oxides, hydrates, solvates, and salts thereof, particularly pharmaceutically acceptable salts thereof, or mixtures of same, for use in the treatment or prophylaxis of diseases, in particular cancer or conditions with dysregulated immune responses or other disorders associated with aberrant AHR signaling.
  • the pharmaceutical activity of the compounds according to the invention can be explained by their activity as AHR inhibitors.
  • the present invention covers the use of compounds of general formula (I), as described supra, or stereoisomers, tautomers, N-oxides, hydrates, solvates, and salts thereof, particularly pharmaceutically acceptable salts thereof, or mixtures of same, for the treatment or prophylaxis of diseases, in particular cancer or conditions with dysregulated immune responses or other disorders associated with aberrant AHR signaling, particularly liquid and solid tumours.
  • the present invention covers the use of a compound of formula (I), described supra, or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, particularly a pharmaceutically acceptable salt thereof, or a mixture of same, for the prophylaxis or treatment of diseases, in particular cancer or conditions with dysregulated immune responses or other disorders associated with aberrant AHR signaling, particularly liquid and solid tumours.
  • the present invention covers the use of compounds of general formula (I), as described supra, or stereoisomers, tautomers, N-oxides, hydrates, solvates, and salts thereof, particularly pharmaceutically acceptable salts thereof, or mixtures of same, in a method of treatment or prophylaxis of diseases, in particular cancer or conditions with dysregulated immune responses or other disorders associated with aberrant AHR signaling, particularly liquid and solid tumours.
  • the present invention covers use of a compound of general formula (I), as described supra, or stereoisomers, tautomers, N-oxides, hydrates, solvates, and salts thereof, particularly pharmaceutically acceptable salts thereof, or mixtures of same, for the preparation of a pharmaceutical composition, preferably a medicament, for the prophylaxis or treatment of diseases, in particular cancer or conditions with dysregulated immune responses or other disorders associated with aberrant AHR signaling, particularly liquid and solid tumours.
  • a pharmaceutical composition preferably a medicament
  • the present invention covers a method of treatment or prophylaxis of diseases, in particular cancer or conditions with dysregulated immune responses or other disorders associated with aberrant AHR signaling, particularly liquid and solid tumours, using an effective amount of a compound of general formula (I), as described supra, or stereoisomers, tautomers, N-oxides, hydrates, solvates, and salts thereof, particularly pharmaceutically acceptable salts thereof, or mixtures of same.
  • a compound of general formula (I) as described supra, or stereoisomers, tautomers, N-oxides, hydrates, solvates, and salts thereof, particularly pharmaceutically acceptable salts thereof, or mixtures of same.
  • the present invention covers pharmaceutical compositions, in particular a medicament, comprising a compound of general formula (I), as described supra, or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, a salt thereof, particularly a pharmaceutically acceptable salt, or a mixture of same, and one or more excipients), in particular one or more pharmaceutically acceptable excipient(s).
  • a compound of general formula (I) as described supra, or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, a salt thereof, particularly a pharmaceutically acceptable salt, or a mixture of same, and one or more excipients), in particular one or more pharmaceutically acceptable excipient(s).
  • excipients in particular one or more pharmaceutically acceptable excipient(s).
  • Conventional procedures for preparing such pharmaceutical compositions in appropriate dosage forms can be utilized.
  • the present invention furthermore covers pharmaceutical compositions, in particular medicaments, which comprise at
  • the compounds according to the invention can have systemic and/or local activity.
  • they can be administered in a suitable manner, such as, for example, via the oral, parenteral, pulmonary, nasal, sublingual, lingual, buccal, rectal, vaginal, dermal, transdermal, conjunctival, otic route or as an implant or stent.
  • a suitable manner such as, for example, via the oral, parenteral, pulmonary, nasal, sublingual, lingual, buccal, rectal, vaginal, dermal, transdermal, conjunctival, otic route or as an implant or stent.
  • the compounds according to the invention can be administered in suitable administration forms.
  • the compounds according to the invention for oral administration, it is possible to formulate the compounds according to the invention to dosage forms known in the art that deliver the compounds of the invention rapidly and/or in a modified manner, such as, for example, tablets (uncoated or coated tablets, for example with enteric or controlled release coatings that dissolve with a delay or are insoluble), orally-disintegrating tablets, films/wafers, films/lyophylisates, capsules (for example hard or soft gelatine capsules), sugar-coated tablets, granules, pellets, powders, emulsions, suspensions, aerosols or solutions. It is possible to incorporate the compounds according to the invention in crystalline and/or amorphised and/or dissolved form into said dosage forms.
  • Parenteral administration can be effected with avoidance of an absorption step (for example intravenous, intraarterial, intracardial, intraspinal or intralumbal) or with inclusion of absorption (for example intramuscular, subcutaneous, intracutaneous, percutaneous or intraperitoneal).
  • absorption step for example intravenous, intraarterial, intracardial, intraspinal or intralumbal
  • absorption for example intramuscular, subcutaneous, intracutaneous, percutaneous or intraperitoneal.
  • Administration forms which are suitable for parenteral administration are, inter alia, preparations for injection and infusion in the form of solutions, suspensions, emulsions, lyophylisates or sterile powders.
  • Examples which are suitable for other administration routes are pharmaceutical forms for inhalation [inter alia powder inhalers, nebulizers], nasal drops, nasal solutions, nasal sprays; tablets/films/wafers/capsules for lingual, sublingual or buccal administration; suppositories; eye drops, eye ointments, eye baths, ocular inserts, ear drops, ear sprays, ear powders, ear-rinses, ear tampons; vaginal capsules, aqueous suspensions (lotions, mixturae agitandae), lipophilic suspensions, emulsions, ointments, creams, transdermal therapeutic systems (such as, for example, patches), milk, pastes, foams, dusting powders, implants or stents.
  • inhalation inter alia powder inhalers, nebulizers
  • nasal drops nasal solutions, nasal sprays
  • tablets/films/wafers/capsules for lingual, sublingual or buccal
  • compositions according to the invention can be incorporated into the stated administration forms. This can be effected in a manner known per se by mixing with pharmaceutically suitable excipients.
  • Pharmaceutically suitable excipients include, inter alia, fillers and carriers (for example cellulose, microcrystalline cellulose (such as, for example, Avicel®), lactose, mannitol, starch, calcium phosphate (such as, for example, Di-Cafos®)), ointment bases (for example petroleum jelly, paraffins, triglycerides, waxes, wool wax, wool wax alcohols, lanolin, hydrophilic ointment, polyethylene glycols), bases for suppositories (for example polyethylene glycols, cacao butter, hard fat), solvents (for example water, ethanol, isopropanol, glycerol, propylene glycol, medium chain-length triglycerides fatty oils, liquid polyethylene glycols, paraffins), surfactants, emuls
  • the present invention furthermore relates to a pharmaceutical composition which comprise at least one compound according to the invention, conventionally together with one or more pharmaceutically suitable excipient(s), and to their use according to the present invention.
  • the present invention covers pharmaceutical combinations, in particular medicaments, comprising at least one compound of general formula (I) of the present invention and at least one or more further active ingredients, in particular for the treatment and/or prophylaxis of cancer or conditions with dysregulated immune responses or other disorders associated with aberrant AHR signalinggeneric name disorders, particularly liquid and solid tumours.
  • the term "combination" in the present invention is used as known to persons skilled in the art, it being possible for said combination to be a fixed combination, a non-fixed combination or a kit-of-parts.
  • a "fixed combination” in the present invention is used as known to persons skilled in the art and is defined as a combination wherein, for example, a first active ingredient, such as one or more compounds of general formula (I) of the present invention, and a further active ingredient are present together in one unit dosage or in one single entity.
  • a “fixed combination” is a pharmaceutical composition wherein a first active ingredient and a further active ingredient are present in admixture for simultaneous administration, such as in a formulation.
  • Another example of a "fixed combination” is a pharmaceutical combination wherein a first active ingredient and a further active ingredient are present in one unit without being in admixture.
  • a non-fixed combination or "kit-of-parts" in the present invention is used as known to persons skilled in the art and is defined as a combination wherein a first active ingredient and a further active ingredient are present in more than one unit.
  • a non-fixed combination or kit-of-parts is a combination wherein the first active ingredient and the further active ingredient are present separately. It is possible for the components of the non-fixed combination or kit-of-parts to be administered separately, sequentially, simultaneously, concurrently or chronologically staggered.
  • the effective dosage of the compounds of the present invention can readily be determined for treatment of each desired indication.
  • the amount of the active ingredient to be administered in the treatment of one of these conditions can vary widely according to such considerations as the particular compound and dosage unit employed, the mode of administration, the period of treatment, the age and sex of the patient treated, and the nature and extent of the condition treated.
  • the total amount of the active ingredient to be administered will generally range from about 0.001 mg/kg to about 200 mg/kg body weight per day, and preferably from about 0.01 mg/kg to about 20 mg/kg body weight per day.
  • Clinically useful dosing schedules will range from one to three times a day dosing to once every four weeks dosing.
  • drug holidays in which a patient is not dosed with a drug for a certain period of time, to be beneficial to the overall balance between pharmacological effect and tolerability. It is possible for a unit dosage to contain from about 0.5 mg to about 1500 mg of active ingredient, and can be administered one or more times per day or less than once a day.
  • the average daily dosage for administration by injection will preferably be from 0.01 to 200 mg/kg of total body weight.
  • the average daily rectal dosage regimen will preferably be from 0.01 to 200 mg/kg of total body weight.
  • the average daily vaginal dosage regimen will preferably be from 0.01 to 200 mg/kg of total body weight.
  • the average daily topical dosage regimen will preferably be from 0.1 to 200 mg administered between one to four times daily.
  • the transdermal concentration will preferably be that required to maintain a daily dose of from 0.01 to 200 mg/kg.
  • the average daily inhalation dosage regimen will preferably be from 0.01 to 100 mg/kg of total body weight.
  • the specific initial and continuing dosage regimen for each patient will vary according to the nature and severity of the condition as determined by the attending diagnostician, the activity of the specific compound employed, the age and general condition of the patient, time of administration, route of administration, rate of excretion of the drug, drug combinations, and the like.
  • the desired mode of treatment and number of doses of a compound of the present invention or a pharmaceutically acceptable salt or ester or composition thereof can be ascertained by those skilled in the art using conventional treatment tests.
  • NMR peak forms are stated as they appear in the spectra, possible higher order effects have not been considered.
  • the multiplicities are stated according to the signal form which appears in the spectrum, NMR-spectroscopic effects of a higher order were not taken into consideration.
  • NMR signals: shift in ppm. Combinations of multiplicity could be e.g. dd doublet from doublet.
  • All reagents, for which the synthesis is not described in the experimental part, are either commercially available, or are known compounds or may be formed from known compounds by known methods by a person skilled in the art.
  • the compounds and intermediates produced according to the methods of the invention may require purification. Purification of organic compounds is well known to the person skilled in the art and there may be several ways of purifying the same compound. In some cases, no purification may be necessary. In some cases, the compounds may be purified by crystallization. In some cases, impurities may be stirred out using a suitable solvent. In some cases, the compounds may be purified by chromatography, particularly flash column chromatography, using for example prepacked silica gel cartridges, e.g.
  • the compounds may be purified by preparative HPLC using for example a Waters autopurifier equipped with a diode array detector and/or on-line electrospray ionization mass spectrometer in combination with a suitable prepacked reverse phase column and eluents such as gradients of water and acetonitrile which may contain additives such as trifluoroacetic acid, formic acid or aqueous ammonia.
  • purification methods as described above can provide those compounds of the present invention which possess a sufficiently basic or acidic functionality in the form of a salt, such as, in the case of a compound of the present invention which is sufficiently basic, a trifluoroacetate or formate salt for example, or, in the case of a compound of the present invention which is sufficiently acidic, an ammonium salt for example.
  • a salt of this type can either be transformed into its free base or free acid form, respectively, by various methods known to the person skilled in the art, or be used as salts in subsequent biological assays. It is to be understood that the specific form (e.g. salt, free base etc.) of a compound of the present invention as isolated and as described herein is not necessarily the only form in which said compound can be applied to a biological assay in order to quantify the specific biological activity.
  • Futher intermediates were prepared in a comparable manner as described by the sequence from intermediate 6 to intermediate 8.
  • Table 2 futher intermediates Inter medi ate structure IUPAC name
  • Starting materials analytics 60 6-(4-chlorophenyl)-2-(3-cyanophenyl)-3-oxo-2,3-dihydropyridazine -4-carboxylic acid Intermediate 5, (3-cyanophenyl)hydr azine
  • Step 1 A flask was charged with 2-(3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.02 g, 4.58 mmol) and molecular sieves (800 mg, 0.4 nm, particle size: ⁇ 50 ⁇ m).
  • Step 2 The material from the first step was dissolved in THF (50.5 mL). Lithium hydroxide (222 mg) in water (2.7 mL) was added and stirred for 3 h at rt. Water (50 mL) was added and the pH was adjusted to pH 6 (3 mL, 2N HCl). The reaction mixture was concentrated to half of its volume. The precipitate was filtered off under suction, washed with water and dried under vacuum at 50°C yielding 340 mg of the title compound which was used without further purification in the next step.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (12)

  1. Composé de formule générale (I) :
    Figure imgb0500
     dans laquelle
    R1 représente hydroxyalkyle en C2-C6, où lesdits groupes hydroxyalkyle en C2-C6 sont facultativement substitués une fois par R7 et facultativement une à trois fois par halogène, ou cycloalkyle en C3-C6 substitué une fois par hydroxy ;
    R2 représente chloro, méthyle, fluorométhyle, difluorométhyle, trifluorométhyle, méthoxy ou difluorométhoxy ;
    R3 représente hydrogène ou méthyle ;
    R4 représente hydrogène ou halogène ;
    R5 représente hydrogène ;
    R6 représente hydrogène ou halogène ;
    R7 représente alcoxy en C1-C4, cycloalkyle en C3-C6, hétérocycloalkyle ou hétéroaryle monocyclique de 4 à 6 chaînons ;
    ses polymorphes, énantiomères, diastéréomères, racémiques, tautomères, N-oxydes, hydrates et solvates, ainsi que ses sels physiologiquement acceptables et des solvates de ces sels, ainsi que des mélanges de ceux-ci.
  2. Composé selon la revendication 1, dans lequel :
    R1 représente hydroxyalkyle en C2-C6, où lesdits groupes hydroxyalkyle en C2-C6 sont facultativement substitués une fois par R7 et facultativement une à trois fois par fluoro ou chloro, ou cycloalkyle en C3-C6 substitué une fois par hydroxy ;
    R2 représente chloro, méthyle, fluorométhyle, difluorométhyle, trifluorométhyle, méthoxy ou difluorométhoxy ;
    R3 représente hydrogène ou méthyle ;
    R4 représente hydrogène, fluoro ou chloro ;
    R5 représente hydrogène ;
    R6 représente hydrogène ou fluoro ;
    R7 représente méthoxy, cyclopropyle, tétrahydrofuranyle, tétrahydropyranyle ou imidazolyle ;
    ses polymorphes, énantiomères, diastéréomères, racémiques, tautomères, N-oxydes, hydrates et solvates, ainsi que ses sels physiologiquement acceptables et des solvates de ces sels, ainsi que des mélanges de ceux-ci.
  3. Composé selon la revendication 1, dans lequel :
    R1 représente hydroxyalkyle en C2-C6, où lesdits groupes hydroxyalkyle en C2-C6 sont facultativement substitués une fois par R7 et facultativement une à trois fois par fluoro ;
    R2 représente chloro, méthyle ou difluorométhyle ;
    R3 représente hydrogène ou méthyle ;
    R4 représente hydrogène, fluoro ou chloro ;
    R5 représente hydrogène ;
    R6 représente hydrogène ou fluoro ;
    R7 représente méthoxy ou tétrahydrofuranyle ;
    ses polymorphes, énantiomères, diastéréomères, racémiques, tautomères, N-oxydes, hydrates et solvates, ainsi que ses sels physiologiquement acceptables et des solvates de ces sels, ainsi que des mélanges de ceux-ci.
  4. Composé selon la revendication 1 ou 2 qui est choisi dans le groupe constitué de :
    2-(3-fluorophényl)-N-(1-hydroxy-3-méthylbutan-2-yl)-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-1-hydroxy-3-méthylbutan-2-yl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthylphényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthylphényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthylphényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(1-hydroxypropan-2-yl)-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-1-hydroxypropan-2-yl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(2-hydroxy-3-méthylbutyl)-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-2-hydroxy-3-méthylbutyl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-2-hydroxy-3-méthylbutyl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(2-hydroxypropyl)-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-2-hydroxypropyl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-2-hydroxypropyl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(2-hydroxy-3-méthoxypropyl)-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-2-hydroxy-3-méthoxypropyl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-2-hydroxy-3-méthoxypropyl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(2-hydroxyéthyl)-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(1-hydroxypropan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(2-hydroxy-3-méthylbutyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-2-hydroxy-3-méthylbutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-2-hydroxy-3-méthylbutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(2-hydroxy-3-méthoxypropyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-2-hydroxy-3-méthoxypropyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-2-hydroxy-3-méthoxypropyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(2-hydroxypropyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-2-hydroxypropyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-2-hydroxypropyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-4-méthylpentan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[2-hydroxy-1-(-tétrahydrofurane-3-yl)éthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-{(1S)-2-hydroxy-1-[(3R)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-{(1S)-2-hydroxy-1-[(3S)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-{(1R)-2-hydroxy-1-[(3R)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-{(1R)-2-hydroxy-1-[(3S)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-difluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-difluorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-difluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-difluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-difluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-difluorophényl)-N-(2-hydroxy-3-méthylbutyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-difluorophényl)-N-[(2S)-2-hydroxy-3-méthylbutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-difluorophényl)-N-[(2R)-2-hydroxy-3-méthylbutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3,5-difluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3,5-difluorophényl)-6-(4-méthylphényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    2-(3,5-difluorophényl)-6-(4-méthylphényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3,5-difluorophényl)-6-(4-méthylphényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3,5-difluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3,5-difluorophényl)-N-(2-hydroxy-3-méthylbutyl)-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3,5-difluorophényl)-N-[(2S)-2-hydroxy-3-méthylbutyl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3,5-difluorophényl)-N-[(2R)-2-hydroxy-3-méthylbutyl]-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-N-[(2S)-1-hydroxy-4-méthylpentan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-N-(1-hydroxypropan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-N-(2-hydroxy-3-méthylbutyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-N-[(2S)-2-hydroxy-3-méthylbutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-chlorophényl)-6-(4-chlorophényl)-N-[(2R)-2-hydroxy-3-méthylbutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    N-(1-hydroxy-3-méthylbutan-2-yl)-6-(4-méthylphényl)-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-6-(4-méthylphényl)-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    N-[(2R)-1-hydroxy-3-méthylbutan-2-yl]-6-(4-méthylphényl)-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    N-(1-hydroxypropan-2-yl)-6-(4-méthylphényl)-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    N-(2-hydroxyéthyl)-6-(4-méthylphényl)-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-3-oxo-2-phényl-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-3-oxo-2-phényl-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-3-oxo-2-phényl-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(1-hydroxypropan-2-yl)-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2R)-1-hydroxypropan-2-yl]-3-oxo-2-phényl-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-(1-hydroxy-3-méthylbutan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-[(2R)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-(1-hydroxybutan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-[(2R)-1-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-(1-hydroxypropan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-diméthylphényl)-2-(3-fluorophényl)-N-[(2R)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhyl)phényl]-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-methylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhyl)phényl]-2-(3-fluorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhyl)phényl]-2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhyl)phényl]-2-(3-fluorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhyl)phényl]-2-(3-fluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhyl)phényl]-2-(3-fluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-3-hydroxypropan-2-yl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[ (2S)-1,1,1-trifluoro-3-hydroxypropan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R)-1,1,1-trifluoro-3-hydroxypropan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthoxyphényl)-3-oxo-N-(-1,1,1-trifluoro-3-hydroxypropan-2-yl)-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthoxyphényl)-3-oxo-N-[(2S)-1,1,1-trifluoro-3-hydroxypropan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthoxyphényl)-3-oxo-N-[(2R)-1,1,1-trifluoro-3-hydroxypropan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(cis-2-hydroxycyclohexyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1R,2S)-2-hydroxycyclohexyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S,2R)-2-hydroxycyclohexyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(cis-2-hydroxycyclohexyl)-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(1R,2S)-2-hydroxycyclohexyl]-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(1S,2R)-2-hydroxycyclohexyl]-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(cis-2-hydroxycyclopentyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-methylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S,2R)-2-hydroxycyclopentyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S,2S)-2-méthylcyclohexyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S,3S)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S,2S)-2-hydroxycyclopentyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S,3S)-3-hydroxybutan-2-yl]-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(trans-2-hydroxycyclohexyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S,2S)-2-hydroxycyclohexyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1R,2R)-2-hydroxycyclohexyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(trans-2-hydroxycyclopentyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1R,2R)-2-hydroxycyclopentyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S,2S)-2-hydroxycyclopentyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthoxyphényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthoxyphényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-6-(4-méthoxyphényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1-hydroxycyclohexyl)méthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-(cis-2-hydroxycyclohexyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S,3S)-1,3-dihydroxybutan-2-yl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-Chlorophényl)-2-(3-fluorophényl)-N-[(1R,2S)-2-hydroxycyclopentyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(3-hydroxybutan-2-yl)-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(1R,2S)-2-hydroxycyclopentyl]-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-(3-hydroxybutan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-[(2S,3S)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-[(2R,3R)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-[(2S,3R)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-[(2R,3S)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-{(2-hydroxy-1-tétrahydrofurane-3-yl)éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-{(1R)-2-hydroxy-1-[(3S)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-{(1R)-2-hydroxy-1-[(3R)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-{(1S)-2-hydroxy-1-[(3R)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-{(1S)-2-hydroxy-1-[(3S)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[2-hydroxy-1-(tétrahydro-2H-pyran-4-yl)éthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1R)-2-hydroxy-1-(tétrahydro-2H-pyran-4-yl)éthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S)-2-hydroxy-1-(tétrahydro-2H-pyran-4-yl)éthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-trans-2-hydroxycyclohexyl-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(trans-2-hydroxycyclopentyl)-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S)-2,3-dihydroxypropyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(1S)-1-cyclopentyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2- (3-fluorophényl)-N-{(2-hydroxy-1-[tétrahydrofurane-3-yl]éthyl}-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2R)-2,3-dihydroxypropyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-(2-hydroxy-3-méthoxypropyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-1-hydroxy-3-(1H-imidazol-5-yl)propan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(1-hydroxy-2-méthylpropan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[1-(hydroxyméthyl)cyclopropyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(2-hydroxy-2-méthylpropyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(3-hydroxypropyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(2-cyclopropyl-2-hydroxyéthyl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2R)-2-cyclopropyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S)-2-cyclopropyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophenyl)-N-(1-cyclopropyl-2-hydroxyethyl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(1R)-1-cyclopropyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(1S)-1-cyclopropyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1-hydroxycyclopropyl)méthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-3-hydroxybutan-2-yl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R,3R)-1,1,1-trifluoro-3-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R,3S)-1,1,1-trifluoro-3-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S,3R)-1,1,1-trifluoro-3-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S,3S)-1,1,1-trifluoro-3-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(3-hydroxy-2-méthylpropyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-3-hydroxy-2-méthylpropyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-3-hydroxy-2-méthylpropyl]-3-oxo-2,3-dihydropyridazine-4-carboxamid ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(3-hydroxybutyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(3R)-3-hydroxybutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(3S)-3-hydroxybutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(4-hydroxybutan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-4-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-4-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(l-cyclobutyl-2-hydroxyéthyl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(1R)-1-cyclobutyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(1S)-1-cyclobutyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1-hydroxycyclobutyl)méthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[1-(hydroxyméthyl)cyclobutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[1-(hydroxyméthyl)cyclopentyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[1-(hydroxyméthyl)cyclohexyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-(4,4,4-trifluoro-3-hydroxybutan-2-yl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R,3R)-4,4,4-trifluoro-3-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S,3R)-4,4,4-trifluoro-3-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R,3S)-4,4,4-trifluoro-3-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S,3S)-4,4,4-trifluoro-3-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(3,3-difluoro-2-hydroxypropyl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2R)-3,3-difluoro-2-hydroxypropyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S)-3,3-difluoro-2-hydroxypropyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(1,4-dihydroxybutan-2-yl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2R)-1,4-dihydroxybutan-2-yl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S)-1,4-dihydroxybutan-2-yl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(1,3-dihydroxypropan-2-yl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthoxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    1,4-anhydro-5-({[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-2,3,5-tridésoxyhexitol ;
    1,4-anhydro-5-({[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-2,3,5-tridésoxy-D-érythro-hexitol ;
    1,4-anhydro-5-({[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-2,3,5-tridésoxy-D-thréo-hexitol ;
    1,4-anhydro-5-({[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-2,3,5-tridésoxy-L-thréo-hexitol ;
    3,6-anhydro-2-({[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-2,4,5-tridésoxy-D-érythro-hexitol ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R,3R)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(2-cyclopentyl-2-hydroxyéthyl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(3-éthyl-2-hydroxypentyl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    N-(1-cyclopropyl-2-hydroxyethyl)-2-(3-fluorophenyl)-6-(4-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-1-hydroxypropan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-methylbutan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-1-hydroxy-3-methylbutan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(2-hydroxy-3-méthylbutyl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-3,3,3-trifluoro-2-hydroxypropyl)-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(3-hydroxy-2-méthylpropyl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-3-hydroxy-2-méthylpropyl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-3-hydroxy-2-méthylpropyl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(3-hydroxybutyl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(3S)-3-hydroxybutyl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(3R)-3-hydroxybutyl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(3-hydroxypropyl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-(1,3-dihydroxypropan-2-yl)-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(4-hydroxybutan-2-yl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-4-hydroxybutan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-4-hydroxybutan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(2-hydroxy-2-méthylpropyl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-methoxypropan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-1-hydroxy-3-methoxypropan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophenyl)-N-(1-hydroxy-4-methoxybutan-2-yl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-1-hydroxy-4-methoxybutan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxy-4-methoxybutan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-3-hydroxybutan-2-yl)-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2R,3R)-1,1,1-trifluoro-3-hydroxybutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2R,3S)-1,1,1-trifluoro-3-hydroxybutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2S,3R)-1,1,1-trifluoro-3-hydroxybutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2S,3S)-1,1,1-trifluoro-3-hydroxybutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-(3,3-difluoro-2-hydroxypropyl)-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-[(2R)-3,3-difluoro-2-hydroxypropyl]-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-[(2S)-3,3-difluoro-2-hydroxypropyl]-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-(1,4-dihydroxybutan-2-yl)-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    1,4-anhydro-2,3,5-tridésoxy-5-[({2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazin-4-yl}carbonyl)amino]hexitol ;
    1,4-anhydro-2,3,5-tridésoxy-5-[ ({2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazin-4-yl}carbonyl)amino]-L-thréo-hexitol ;
    1,4-anhydro-2,3,5-tridésoxy-5-[ ({2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazin-4-yl}carbonyl)amino]-D-thréo-hexitol ;
    3,6-anhydro-2,4,5-tridésoxy-2-[({2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazin-4-yl}carbonyl)amino]-D-érythro-hexitol ;
    1,4-anhydro-2,3,5-tridésoxy-5-[({2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazin-4-yl}carbonyl)amino]-D-érythro-hexitol ;
    N-[(2S)-2,3-dihydroxypropyl]-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-[(2R)-2,3-dihydroxypropyl]-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-3-hydroxypropan-2-yl)-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-(1-cyclopropyl-2-hydroxyéthyl)-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-[(1R)-1-cyclopropyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    N-[(1S)-1-cyclopropyl-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-(4,4,4-trifluoro-3-hydroxybutan-2-yl)-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2R,3R)-4,4,4-trifluoro-3-hydroxybutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2S,3R)-4,4,4-trifluoro-3-hydroxybutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2R,3S)-4,4,4-trifluoro-3-hydroxybutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2S,3S)-4,4,4-trifluoro-3-hydroxybutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3,3-diméthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-3-hydroxy-3-méthylbutan-2-yl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R)-1,1,1-trifluoro-3-hydroxy-3-méthylbutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S)-1,1,1-trifluoro-3-hydroxy-3-méthylbutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[1,1,1-trifluoro-3-hydroxy-2-(hydroxyméthyl)propan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-3-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-3-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhyl)phényl]-2-(3-fluorophényl)-3-oxo-N-[(2R)-1,1,1-trifluoro-3-hydroxypropan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-6-(4-méthoxyphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-dichlorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-dichlorophényl)-N-[2-hydroxy-1-(tétrahydrofurane-3-yl)éthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-dichlorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3,5-dichlorophényl)-N-[(2S,3S)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-1-hydroxy-3-méthoxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[2-(1-hydroxycyclohexyl)éthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(3-hydroxy-3-méthylbutyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(2,3-dihydroxy-3-méthylbutyl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2RS)-1-fluoro-3-hydroxypropan-2-yl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(cis-3-hydroxycyclobutyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(4-hydroxytétrahydro-2H-pyran-4-yl)méthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1-hydroxycyclopentyl)méthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(3-hydroxyoxetan-3-yl)méthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2RS)-1-hydroxy-3-(pyridin-2-yl)propan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2RS)-1-hydroxy-3-(pyridin-4-yl)propan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(trans-2-hydroxycyclobutyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S,2S)-2-hydroxycyclobutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1R,2R)-2-hydroxycyclobutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(3,4-dihydroxybutan-2-yl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S,3S)-3,4-dihydroxybutan-2-yl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S,3R)-3,4-dihydroxybutan-2-yl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2R,3S)-3,4-dihydroxybutan-2-yl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2R,3R)-3,4-dihydroxybutan-2-yl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[1-hydroxy-3-(pyridin-3-yl)propan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-4-hydroxybutan-2-yl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S)-1,1,1-trifluoro-4-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R)-1,1,1-trifluoro-4-hydroxybutan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(cis-2-hydroxycyclobutyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1R,2S)-2-hydroxycyclobutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(1S,2R)-2-hydroxycyclobutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhyl)phényl]-2-(3-fluorophényl)-N-[(2S)-3-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[4-(difluorométhoxy)phényl]-2-(3-fluorophényl)-N-[(2S)-3-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-3-hydroxy-1-isopropoxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-3-hydroxy-3-méthylbutan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-3-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-3-hydroxy-3-méthylbutan-2-yl)-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2R)-1,1,1-trifluoro-3-hydroxy-3-méthylbutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2S)-1,1,1-trifluoro-3-hydroxy-3-méthylbutan-2-yl]-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide
    et
    6-[4-(fluorométhyl)phényl]-2-(3-fluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    leurs polymorphes, énantiomères, diastéréomères, racémiques, tautomères, N-oxydes, hydrates et solvates, ainsi que leurs sels physiologiquement acceptables et des solvates de ces sels, ainsi que des mélanges de ceux-ci.
  5. Composé qui est choisi dans le groupe constitué de :
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-(trans-4-hydroxytétrahydrofuran-3-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    N-{[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}-L-sérinate de méthyle ;
    N-[(2S)-1-amino-3-hydroxy-1-oxopropan-2-yl]-6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    N-(4-amino-1-hydroxy-4-oxobutan-2-yl)-6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    N-{[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}-L-sérine ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(3S,4S)-4-hydroxytétrahydrofuran-3-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(3S,4R)-4-hydroxytétrahydrofuran-3-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(3R,4S)-4-hydroxytétrahydrofuran-3-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-3-hydroxypropan-2-yl)-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2R)-1,1,1-trifluoro-3-hydroxypropan-2-yl]-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2S)-1,1,1-trifluoro-3-hydroxypropan-2-yl]-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[2-hydroxy-1-(tétrahydrofurane-3-yl)éthyl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-{(1R)-2-hydroxy-1-[(3S)-tétrahydrofurane-3-yl]éthyl}-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-{(1R)-2-hydroxy-1-[(3R)-tétrahydrofurane-3-yl]éthyl}-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-{(1S)-2-hydroxy-1-[(3R)-tétrahydrofurane-3-yl]éthyl}-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-{(1S)-2-hydroxy-1-[(3S)-tétrahydrofurane-3-yl]éthyl}-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(3-hydroxybutan-2-yl)-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R,3R)-3-hydroxybutan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S,3R)-3-hydroxybutan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R,3S)-3-hydroxybutan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S,3S)-3-hydroxybutan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2R)-1-hydroxy-3-phénylpropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-phénylpropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(4-hydroxy-1-méthylpipéridin-4-yl)méthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[3-(diméthylamino)-2-hydroxypropyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-phénylpropan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-1-hydroxy-3-phénylpropan-2-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    1,5-anhydro-2-({[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-2,4-didésoxy-D-érythro-pentitol ;
    6-(4-chlorophényl)-N-[(trans)-3,3-difluoro-2-hydroxycyclohexyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(1R,2S)-3,3-difluoro-2-hydroxycyclohexyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(1S,2R)-3,3-difluoro-2-hydroxycyclohexyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    N-{[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}-D-sérinate de méthyle ;
    2-(3-fluorophényl)-N-(cis-4-hydroxytétrahydrofuran-3-yl)-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(3R,4R)-4-hydroxytétrahydrofuran-3-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(3S,4S)-4-hydroxytétrahydrofuran-3-yl]-3-oxo-6-[4-(trifluorométhyl)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-cyanophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-cyanophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-cyanophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-cyanophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-2-(3-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-méthylphényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-méthylphényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-méthylphényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-2-(3-méthylphényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-[3-(difluorométhyl)phényl]-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-(1-cyano-2-hydroxyéthyl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(trans-3-hydroxycyclobutyl)méthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[3-chloro-4-(diméthylamino)phényl]-2-(3-fluorophényl)-3-oxo-N-[(2R)-1,1,1-trifluoro-3-hydroxypropan-2-yl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-6-[4-(morpholin-4-yl)phényl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[3-chloro-4-(diméthylamino)phényl]-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-[3-chloro-4-(diméthylamino)phényl]-2-(3-fluorophényl)-3-oxo-N-(1,1,1-trifluoro-3-hydroxypropan-2-yl)-2,3-dihydropyridazine-4-carboxamide ;
    6-[3-chloro-4-(diméthylamino)phényl]-2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    2- (3-fluorophényl)-N-[(trans)-4-hydroxytétrahydrofuran-3-yl]-6-[4-(morpholin-4-yl)phényl]-3- oxo-2,3-dihydropyridazine-4-carboxamide ;
    N-[(1S)-1-cyclopropyl-2-hydroxy-2-méthylpropyl]-2-(3-fluorophényl)-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2S)-3-hydroxy-3-méthylbutan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-[(2R)-3-hydroxy-3-méthylbutan-2-yl]-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    2-(3-fluorophényl)-N-(2-hydroxy-2-méthylpropyl)-3-oxo-6-[4-(trifluorométhoxy)phényl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[cis-4-hydroxytétrahydrofuran-3-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[(3R,4R)-4-hydroxytétrahydrofuran-3-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    (3R,4S)-3-({ [6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-4-hydroxypyrrolidine-1-carboxylate de tert-butyle ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[cis-4-hydroxy-1-méthylpyrrolidin-3-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-[3-(difluorométhyl)phényl]-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-N-[(1S)-1-cyano-2-hydroxyéthyl]-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chlorophényl)-2-(3-fluorophényl)-N-[trans-3-(hydroxyméthyl)cyclobutyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    3-({[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-2,2-diméthylpropanoate de méthyle ;
    acide 3-({[6-(4-chlorophényl)-2-(3-fluorophényl)-3-oxo-2,3-dihydropyridazin-4-yl]carbonyl}amino)-2,2-diméthylpropanoïque ;
    6-(4-chlorophényl)-2-(3-cyanophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-[2-hydroxy-1-(tétrahydrofurane-3-yl)éthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-{(1R)-2-hydroxy-1-[(3R)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-{(1S)-2-hydroxy-1-[(3S)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-{(1S)-2-hydroxy-1-[(3R)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-{(1R)-2-hydroxy-1-[(3S)-tétrahydrofurane-3-yl]éthyl}-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-(3-hydroxybutan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-[(2S,3S)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3-fluorophényl)-N-(cis-2-hydroxycyclohexyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-N-(2-hydroxy-3-méthoxypropyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-N-(3-hydroxybutan-2-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-N-[(2S,3S)-3-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-N-[(2S)-1-hydroxybutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(3,4-dichlorophényl)-2-(3-fluorophényl)-N-[2-hydroxy-1-(tétrahydrofurane-3-yl)éthyl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3,5-difluorophényl)-N-[(2S)-1-hydroxy-3-méthylbutan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3,5-difluorophényl)-N-[(2S)-1-hydroxypropan-2-yl]-3-oxo-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3,5-difluorophényl)-3-oxo-N-(3,3,3-trifluoro-2-hydroxypropyl)-2,3-dihydropyridazine-4-carboxamide ;
    6-(4-chloro-3-fluorophényl)-2-(3,5-difluorophényl)-3-oxo-N-[(2R)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    et
    6-(4-chloro-3-fluorophényl)-2-(3,5-difluorophényl)-3-oxo-N-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,3-dihydropyridazine-4-carboxamide ;
    leurs polymorphes, énantiomères, diastéréomères, racémiques, tautomères, N-oxydes, hydrates et solvates, ainsi que leurs sels physiologiquement acceptables et des solvates de ces sels, ainsi que des mélanges de ceux-ci.
  6. Procédé de préparation d'un composé de formule générale (I) selon l'une quelconque des revendications 1 à 4, ledit procédé comprenant l'étape consistant à amener un composé intermédiaire de formule générale (VII) :
    Figure imgb0501
     dans laquelle R2, R3, R4, R5 et R6 sont tels que définis pour le composé de formule générale (I) selon l'une quelconque des revendications 1 à 3, à réagir avec un composé de formule générale (VIII) :

            H2N-R1     (III),

    dans laquelle R1 est tel que défini pour le composé de formule générale (I) selon l'une quelconque des revendications 1 à 3,
    de façon à obtenir un composé de formule générale (I) :
    Figure imgb0502
     dans laquelle R1, R2, R3, R4, R5 et R6 sont tels que définis pour le composé de formule générale (I) selon l'une quelconque des revendications 1 à 3.
  7. Composé de formule générale (I) selon l'une quelconque des revendications 1 à 4 ou composé selon la revendication 5 pour le traitement d'une maladie.
  8. Composition pharmaceutique comprenant un composé de formule générale (I) selon l'une quelconque des revendications 1 à 4 ou un composé selon la revendication 5 et un ou plusieurs excipients pharmaceutiquement acceptables.
  9. Combinaison pharmaceutique comprenant :
    • une ou plusieurs premières substances actives, des composés de formule générale (I} selon l'une quelconque des revendications 1 à 4 ou un composé selon la revendication 5,
    et
    • un ou plusieurs composés anticancéreux pharmaceutiquement actifs ou
    • un ou plusieurs inhibiteurs de point de contrôle immunitaire pharmaceutiquement actifs.
  10. Composé de formule générale (I) selon l'une quelconque des revendications 1 à 4 ou composé selon la revendication 5 pour utilisation en tant que médicament.
  11. Composé de formule générale (VII) :
    Figure imgb0503
     dans laquelle R2, R3, R4, R5 et R6 sont tels que définis pour le composé de formule générale (I) selon l'une quelconque des revendications 1 à 3.
  12. Utilisation d'un composé de formule générale (VII)
    Figure imgb0504
     dans laquelle R2, R3, R4, R5 et R6 sont tels que définis pour le composé de formule générale (I) selon l'une quelconque des revendications 1 à 3, pour la préparation d'un composé de formule générale (I) selon l'une quelconque des revendications 1 à 4.
EP17724833.3A 2016-05-25 2017-05-23 3-oxo-2,6-diphényl-2,3-dihydropyridazine-4-carboxamides Active EP3464248B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN2016083308 2016-05-25
CN2017074408 2017-02-22
PCT/EP2017/062355 WO2017202816A1 (fr) 2016-05-25 2017-05-23 3-oxo-2,6-diphényl-2,3-dihydropyridazine-4-carboxamides

Publications (2)

Publication Number Publication Date
EP3464248A1 EP3464248A1 (fr) 2019-04-10
EP3464248B1 true EP3464248B1 (fr) 2021-09-08

Family

ID=58745251

Family Applications (1)

Application Number Title Priority Date Filing Date
EP17724833.3A Active EP3464248B1 (fr) 2016-05-25 2017-05-23 3-oxo-2,6-diphényl-2,3-dihydropyridazine-4-carboxamides

Country Status (27)

Country Link
US (1) US11040035B2 (fr)
EP (1) EP3464248B1 (fr)
JP (1) JP6964096B2 (fr)
KR (1) KR20190009369A (fr)
CN (1) CN109863140B (fr)
AU (1) AU2017269870A1 (fr)
BR (1) BR112018074185A2 (fr)
CA (1) CA3025227A1 (fr)
CL (1) CL2018003345A1 (fr)
CO (1) CO2018012654A2 (fr)
CR (1) CR20180556A (fr)
CU (1) CU20180143A7 (fr)
DO (1) DOP2018000256A (fr)
EA (1) EA201892666A1 (fr)
EC (1) ECSP18087725A (fr)
IL (1) IL263046A (fr)
MA (1) MA45087A (fr)
MX (1) MX2018014443A (fr)
NI (1) NI201800124A (fr)
PE (1) PE20190509A1 (fr)
PH (1) PH12018502472A1 (fr)
SG (1) SG11201810366WA (fr)
SV (1) SV2018005787A (fr)
TN (1) TN2018000392A1 (fr)
TW (1) TW201742859A (fr)
UY (1) UY37256A (fr)
WO (1) WO2017202816A1 (fr)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI759301B (zh) 2016-05-24 2022-04-01 美商安美基公司 聚乙二醇化卡非佐米化合物
JOP20190193A1 (ar) * 2017-02-09 2019-08-08 Bayer Pharma AG ممركبات 2-أريل غير متجانس-3-أكسو-2، 3-ثنائي هيدرو بيريدازين-4-كربوكساميد لمعالجة السرطان
US11459312B2 (en) 2017-11-21 2022-10-04 Bayer Aktiengesellschaft Sulphur substituted 3-oxo-2,3-dihydropyridazine-4-carboxamides
EP3713931A1 (fr) * 2017-11-21 2020-09-30 Bayer Aktiengesellschaft 3-oxo-6-hétéroaryl-2-phényl-2,3-dihydropyridazine-4-carboxamides
EA037978B1 (ru) * 2017-11-21 2021-06-18 Байер Акциенгезельшафт 2-гетероарил-3-оксо-2,3-дигидропиридазин-4-карбоксамиды для лечения злокачественного новообразования
WO2019101647A1 (fr) * 2017-11-21 2019-05-31 Bayer Aktiengesellschaft 2-phénylpyrimidine-4-carboxamides à utiliser en tant qu'inhibiteurs d'ahr
BR112021003529A2 (pt) 2018-08-24 2021-05-18 Jaguahr Therapeutics Pte Ltd derivados de tetra-hidropiridopirimidina como moduladores de ahr
EP3843853A1 (fr) 2018-08-31 2021-07-07 Jaguahr Therapeutics Pte Ltd Composés hétérocycliques en tant que modulateurs de l'ahr
CN109771437B (zh) * 2019-03-28 2023-03-17 西安交通大学医学院第一附属医院 三氟胸苷在制备治疗三阴性乳腺癌药物中的应用
EP3715471A1 (fr) 2019-03-29 2020-09-30 Deutsches Krebsforschungszentrum, Stiftung des öffentlichen Rechts Ensemble de marqueur de signature d'ahr
EP3721894A1 (fr) 2019-04-10 2020-10-14 Deutsches Krebsforschungszentrum, Stiftung des öffentlichen Rechts Gène 1 induit par l'interleukine-4 (il4i1) en tant que biomarqueur et ses utilisations
EP4005637A4 (fr) * 2019-07-29 2023-07-19 Takeda Pharmaceutical Company Limited Composé hétérocyclique
EP3835432A1 (fr) 2019-12-10 2021-06-16 Deutsches Krebsforschungszentrum, Stiftung des öffentlichen Rechts Gène 1 induit par l'interleukine-4 (il4i1) et métabolites respectifs en tant que biomarqueurs pour le cancer
CN114786674A (zh) * 2019-12-16 2022-07-22 拜耳公司 Ahr抑制剂和pd1抑制剂抗体的组合及其在癌症治疗中的用途
MX2022008532A (es) 2020-01-10 2022-09-09 Ikena Oncology Inc Inhibidores de hidrocarburo de arilo (ahr) y usos de estos.
WO2021173082A1 (fr) 2020-02-26 2021-09-02 Jaguahr Therapeutics Pte Ltd Dérivés de pyridopyrimidine utiles dans la modulation de la signalisation de l'ahr
MX2022011826A (es) * 2020-03-27 2022-10-18 Dong A St Co Ltd Derivados de aminopirimidina y su uso como moduladores del receptor de hidrocarburos de arilo.
US11911376B2 (en) 2020-03-30 2024-02-27 The Regents Of The University Of Colorado Methods for preventing and treating retinal damage
CN114181212B (zh) * 2020-09-15 2023-06-06 山东轩竹医药科技有限公司 哒嗪酮类AhR抑制剂
WO2022078356A1 (fr) * 2020-10-15 2022-04-21 山东轩竹医药科技有限公司 Inhibiteur d'ahr hétéroaromatique
CN114685426A (zh) * 2020-12-28 2022-07-01 苏州泽璟生物制药股份有限公司 磺酰胺类抑制剂及其制备方法和应用
CN118234710A (zh) * 2021-09-14 2024-06-21 元启(苏州)生物制药有限公司 2-芳基或杂芳基-3-氧代-4-甲酰胺-6-环-二氢吡嗪芳基烃受体调节剂和其在治疗疾病和病症中的用途
WO2024076300A1 (fr) 2022-10-03 2024-04-11 Jaguahr Therapeutics Pte Ltd Composés utiles dans la modulation de la signalisation d'ahr

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4134467A1 (de) 1991-10-18 1993-04-22 Thomae Gmbh Dr K Heterobiarylderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung
US6469003B1 (en) * 1998-08-14 2002-10-22 Nihon Nohyaku Co., Ltd. Pyridazinone derivatives
US20030225081A1 (en) * 2000-09-18 2003-12-04 Satoshi Nagato Pyridazinones and triazinones and medicinal use thereof
FR2847253B1 (fr) 2002-11-19 2007-05-18 Aventis Pharma Sa Nouveaux derives de pyridazinones a titre de medicaments et compositions pharmaceutiques les renfermant
FR2847235B1 (fr) 2002-11-20 2005-07-08 Essilor Int Emballage de protection et de calage pour objets a contour circulaire
AR057986A1 (es) * 2005-11-21 2008-01-09 Japan Tobacco Inc Compuesto heterociclico y su uso farmaceutico
EP2328586A2 (fr) 2008-05-20 2011-06-08 Cephalon, Inc. Dérivés pyridazinone substitués comme ligands des récepteurs de l'histamine-3 (h3)
PE20100362A1 (es) 2008-10-30 2010-05-27 Irm Llc Derivados de purina que expanden las celulas madre hematopoyeticas
CN103179968B (zh) 2010-07-27 2017-10-03 波士顿大学管理委员会 作为癌症疗法的芳烃受体(AhR)调节剂
US20170173008A1 (en) 2014-03-19 2017-06-22 President And Fellows Of Harvard College Antimicrobial agents and screening methods

Also Published As

Publication number Publication date
SV2018005787A (es) 2019-02-07
US11040035B2 (en) 2021-06-22
TN2018000392A1 (en) 2020-06-15
TW201742859A (zh) 2017-12-16
CO2018012654A2 (es) 2018-12-14
SG11201810366WA (en) 2018-12-28
IL263046A (en) 2018-12-31
EA201892666A1 (ru) 2019-08-30
UY37256A (es) 2018-01-02
ECSP18087725A (es) 2018-11-30
NI201800124A (es) 2019-04-29
DOP2018000256A (es) 2019-02-15
CU20180143A7 (es) 2019-07-04
MA45087A (fr) 2021-05-26
BR112018074185A2 (pt) 2019-03-06
CA3025227A1 (fr) 2017-11-30
US20200237757A1 (en) 2020-07-30
CN109863140A (zh) 2019-06-07
CN109863140B (zh) 2023-02-21
MX2018014443A (es) 2019-04-15
PH12018502472A1 (en) 2019-09-23
PE20190509A1 (es) 2019-04-10
AU2017269870A1 (en) 2018-12-06
JP6964096B2 (ja) 2021-11-10
JP2019516744A (ja) 2019-06-20
CR20180556A (es) 2019-04-23
WO2017202816A1 (fr) 2017-11-30
EP3464248A1 (fr) 2019-04-10
CL2018003345A1 (es) 2019-03-15
KR20190009369A (ko) 2019-01-28

Similar Documents

Publication Publication Date Title
EP3464248B1 (fr) 3-oxo-2,6-diphényl-2,3-dihydropyridazine-4-carboxamides
EP3580211B1 (fr) 2-hétéroaryl-3-oxo-2,3-dihydropyridazine-4-carboxamides pour le traitement du cancer
US11459312B2 (en) Sulphur substituted 3-oxo-2,3-dihydropyridazine-4-carboxamides
EP3713926B1 (fr) 4-carboxamides de 2-hetarylpyrimidine comme des antagonistes de l'aryl hydrocarbon receptor
US11591311B2 (en) 3-oxo-6-heteroaryl-2-phenyl-2,3-dihydropyridazine-4-carboxamides
EP3713923B1 (fr) 2-phénylpyrimidine-4-carboxamides à utiliser en tant qu'inhibiteurs d'ahr
EA037978B1 (ru) 2-гетероарил-3-оксо-2,3-дигидропиридазин-4-карбоксамиды для лечения злокачественного новообразования

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20190102

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

RAV Requested validation state of the european patent: fee paid

Extension state: MA

Effective date: 20190102

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20200114

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602017045653

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: C07D0237160000

Ipc: A61K0031500000

RIC1 Information provided on ipc code assigned before grant

Ipc: A61P 43/00 20060101ALI20210319BHEP

Ipc: A61P 37/06 20060101ALI20210319BHEP

Ipc: A61P 37/02 20060101ALI20210319BHEP

Ipc: A61P 35/00 20060101ALI20210319BHEP

Ipc: C07D 403/12 20060101ALI20210319BHEP

Ipc: C07D 405/12 20060101ALI20210319BHEP

Ipc: C07D 237/20 20060101ALI20210319BHEP

Ipc: C07D 237/16 20060101AFI20210319BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

RIC1 Information provided on ipc code assigned before grant

Ipc: A61P 37/02 20060101ALI20210408BHEP

Ipc: A61P 35/00 20060101ALI20210408BHEP

Ipc: C07D 403/12 20060101ALI20210408BHEP

Ipc: C07D 405/12 20060101ALI20210408BHEP

Ipc: C07D 237/20 20060101ALI20210408BHEP

Ipc: C07D 237/16 20060101ALI20210408BHEP

Ipc: A61P 37/06 20060101ALI20210408BHEP

Ipc: A61P 43/00 20060101ALI20210408BHEP

Ipc: A61K 31/50 20060101AFI20210408BHEP

INTG Intention to grant announced

Effective date: 20210503

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1427952

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210915

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602017045653

Country of ref document: DE

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20210908

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211208

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211208

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1427952

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210908

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211209

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220108

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220110

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602017045653

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

26N No opposition filed

Effective date: 20220609

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20220531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220523

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220523

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230507

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20170523

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

VS25 Lapsed in a validation state [announced via postgrant information from nat. office to epo]

Ref country code: MA

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20240418

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20240416

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20240422

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210908